Smith-Perry Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Smith-Perry Corp. makes
Smith-Perry Corp. manufactures the VOYAGER PX and VOYAGER/X, which are medical devices designed for use in vascular procedures, including peripheral and coronary interventions.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Voyager Px Ref K895082
Regimes: 510(k) Registry: 510(k)Voyager/X Ref K884754
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Smith-Perry Corp. have in the registry?
The registry currently lists 2 devices for Smith-Perry Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smith-Perry Corp.'s devices?
Among its 2 most recently registered devices, Smith-Perry Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Smith-Perry Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Smith-Perry Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Smith-Perry Corp. in the registry?
The most recently registered devices listed for Smith-Perry Corp. include VOYAGER PX and VOYAGER/X.